HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619322Generated: October 26, 2026
Methyl iodide → 1-Tert-butyl 2-methyl 2-methylpyrrolidine-1,2-dicarboxylate
https://huagongshe.com/reaction/1619322
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-Tert-butoxycarbonyl-2-methyl-pyrrolidine-2-carboxylate | HCID 71744148 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Tert-butyl 2-methyl 2-methylpyrrolidine-1,2-dicarboxylate | HCID 23512223 | 63.2% |
Reaction Steps
To a solution of diisopropylamine (1.59 g, 15.7 mmol) in THF (10 mL) was added n-BuLi (7.54 mL, 2.5 M in n-hexane) dropwise at 0° C. Then the solution was stirred at the same temperature for 30 min. 1-tert-butyl 2-methylpyrrolidine-1,2-dicarboxylate (3.0 g, 13.0 mmol) was dissolved in 50 mL THF and cooled to −78° C. To the solution was added prepared lithium diisopropylamide (15.7 mmol) dropwise. After the reaction mixture was kept at −78° C. for 3 h, MeI (1.6 mL, 25.7 mmol) was added. The mixture was allowed to warm to 0° C. and stirred for 2 h. Then the reaction mixture was quenched with water (30 mL) and extracted with EtOAc (3×50 mL). The combined organic layers were dried over Na2SO4 and concentrated under vacuum to give 2 g of the crude product. MS (ESI): 244 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772301B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-f4ec1eef9f0248f9931a5b711caeb566 |
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| Source note | uspto-grants-2014_07 |
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